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补丁增强型肩袖手术(PARCS)可行性研究的研究方案。

Patch-augmented rotator cuff surgery (PARCS) study-protocol for a feasibility study.

作者信息

Cook Jonathan A, Merritt Naomi, Rees Jonathan L, Crocker Joanna C, Hopewell Sally, Dritsaki Melina, Beard David J, Rangan Amar, Cooper Cushla, Kottam Lucksy, Farrar-Hockley Dair, Thomas Michael, Earle Robert, Carr Andrew J

机构信息

1Centre for Statistics in Medicine, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.

2NIHR Oxford Biomedical Research Centre, Nuffield Department of Orthopaedics, Rheumatology and Musculoskeletal Sciences, University of Oxford, Oxford, UK.

出版信息

Pilot Feasibility Stud. 2018 Dec 21;4:188. doi: 10.1186/s40814-018-0380-7. eCollection 2018.

Abstract

BACKGROUND

A rotator cuff tear is a common disabling shoulder problem. Symptoms include pain, weakness, lack of shoulder mobility and sleep disturbance. Many patients require surgery to repair the tear; however, there is a high failure rate. There is a pressing need to improve the outcome of rotator cuff surgery and the use of patch augmentation to provide support to the healing process and improve patient outcomes holds new promise. Patches have been made using different materials (e.g. human/animal skin or intestine tissue, and completely synthetic materials) and processes (e.g. woven or a mesh). However, clinical evidence on their use is limited. The aim of the patch-augmented rotator cuff surgery (PARCS) feasibility study is to determine, using a mixed method approach, the design of a definitive randomised trial assessing the effectiveness and cost-effectiveness of a patch to augment surgical repair of the rotator cuff that is both acceptable to stakeholders and feasible.

METHODS

The objectives of this six-stage mixed methods feasibility study are to determine current practice, evidence and views about patch use; achieve consensus on the design of a randomised trial to evaluate patch-augmented rotator cuff surgery; and assess the acceptability and feasibility of the proposed design. The six stages will involve a systematic review of clinical evidence, two surveys of surgeons, focus groups and interviews with stakeholders, a Delphi study and a consensus meeting. The various stakeholders (including patients, surgeons, and representatives from industry, the NHS and regulatory bodies) will be involved across the six stages.

DISCUSSION

The PARCS feasibility study will inform the feasibility and acceptability of a randomised trial of the effectiveness and cost-effectiveness of a patch-augmented rotator cuff surgery. Consensus opinion on the basic design of a randomised trial will be sought.

TRIAL REGISTRATION

Not applicable.

摘要

背景

肩袖撕裂是一种常见的导致肩部功能障碍的问题。症状包括疼痛、无力、肩部活动受限和睡眠障碍。许多患者需要手术修复撕裂;然而,失败率很高。迫切需要改善肩袖手术的效果,使用补片增强来支持愈合过程并改善患者预后带来了新的希望。补片已采用不同材料(如人/动物皮肤或肠组织,以及完全合成材料)和工艺(如编织或网状)制成。然而,关于其使用的临床证据有限。补片增强肩袖手术(PARCS)可行性研究的目的是采用混合方法确定一项确定性随机试验的设计,该试验评估补片增强肩袖手术修复的有效性和成本效益,且该设计对利益相关者来说是可接受且可行的。

方法

这项六阶段混合方法可行性研究的目标是确定关于补片使用的当前实践、证据和观点;就评估补片增强肩袖手术的随机试验设计达成共识;并评估所提议设计的可接受性和可行性。这六个阶段将包括对临床证据的系统评价、对外科医生的两项调查、焦点小组讨论以及与利益相关者的访谈、德尔菲研究和一次共识会议。六个阶段都将有不同的利益相关者(包括患者、外科医生以及来自行业、英国国家医疗服务体系和监管机构的代表)参与。

讨论

PARCS可行性研究将为补片增强肩袖手术有效性和成本效益的随机试验的可行性和可接受性提供信息。将寻求关于随机试验基本设计的共识意见。

试验注册

不适用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d155/6302398/6aa9b279cf7b/40814_2018_380_Fig1_HTML.jpg

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